Canonical Allele Identifier: CA633401887
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1441606846
gnomAD v2: 19-47507631-AC-A
gnomAD v3: 19-47004374-AC-A
gnomAD v4: 19-47004374-AC-A
MyVariant Identifiers: chr19:g.47507632del (hg19) chr19:g.47004375del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004376del , CM000681.2:g.47004376del GRCh38
NC_000019.9:g.47507633del , CM000681.1:g.47507633del GRCh37
NC_000019.8:g.52199473del NCBI36
NG_047014.1:g.90810del
NG_047014.2:g.148380del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8188del ENSP00000385720.2:n.8188del
ENST00000672722.1:c.*3688del MANE Select ENSP00000500409.1:n.*3688del
ENST00000404338.7:c.8188del ENSP00000385720.2:n.8188del
NM_004491.4:c.8188del NP_004482.4:n.8188del
NM_004491.5:c.*3688del MANE Select NP_004482.4:n.*3688del
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